Other mutations in this stock |
Total: 86 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc6 |
A |
T |
7: 45,652,025 (GRCm39) |
M614K |
probably benign |
Het |
Adamts7 |
G |
T |
9: 90,075,918 (GRCm39) |
V1217L |
probably null |
Het |
Adcyap1r1 |
T |
A |
6: 55,458,100 (GRCm39) |
N300K |
probably damaging |
Het |
Atf7ip |
A |
G |
6: 136,576,648 (GRCm39) |
D1017G |
probably damaging |
Het |
Atg2b |
A |
C |
12: 105,605,500 (GRCm39) |
D1488E |
probably damaging |
Het |
Atxn2 |
A |
G |
5: 121,933,091 (GRCm39) |
T805A |
probably benign |
Het |
Azi2 |
A |
T |
9: 117,884,960 (GRCm39) |
H223L |
probably benign |
Het |
Banp |
T |
A |
8: 122,727,852 (GRCm39) |
S349T |
probably damaging |
Het |
Bicra |
A |
T |
7: 15,705,875 (GRCm39) |
I1522N |
probably damaging |
Het |
Brca2 |
A |
T |
5: 150,472,126 (GRCm39) |
R2342* |
probably null |
Het |
C6 |
T |
C |
15: 4,822,622 (GRCm39) |
C623R |
probably damaging |
Het |
Cc2d2a |
T |
C |
5: 43,860,645 (GRCm39) |
Y574H |
possibly damaging |
Het |
Cdk5rap3 |
C |
T |
11: 96,803,212 (GRCm39) |
C115Y |
probably benign |
Het |
Chrm4 |
T |
A |
2: 91,758,033 (GRCm39) |
M147K |
probably benign |
Het |
Cit |
A |
T |
5: 115,984,442 (GRCm39) |
K5* |
probably null |
Het |
Ciz1 |
T |
A |
2: 32,260,262 (GRCm39) |
S231T |
probably benign |
Het |
Crebrf |
A |
G |
17: 26,961,520 (GRCm39) |
I206V |
probably benign |
Het |
Cyc1 |
T |
C |
15: 76,227,863 (GRCm39) |
S34P |
probably benign |
Het |
Dnah5 |
A |
G |
15: 28,388,097 (GRCm39) |
I3185M |
probably benign |
Het |
Dtnbp1 |
T |
C |
13: 45,075,702 (GRCm39) |
D347G |
unknown |
Het |
Dzip3 |
A |
T |
16: 48,751,628 (GRCm39) |
V767E |
probably damaging |
Het |
Gdf3 |
A |
T |
6: 122,583,279 (GRCm39) |
C363S |
probably damaging |
Het |
Glb1l |
T |
C |
1: 75,176,975 (GRCm39) |
K487R |
probably damaging |
Het |
Gm9747 |
T |
C |
1: 82,212,002 (GRCm39) |
V67A |
unknown |
Het |
Hoxb2 |
A |
G |
11: 96,242,736 (GRCm39) |
T34A |
possibly damaging |
Het |
Ifnk |
C |
T |
4: 35,152,383 (GRCm39) |
R104C |
probably damaging |
Het |
Igfbp1 |
A |
T |
11: 7,151,952 (GRCm39) |
I252F |
probably damaging |
Het |
Ighv1-74 |
T |
C |
12: 115,766,480 (GRCm39) |
T47A |
probably benign |
Het |
Igkv4-62 |
A |
T |
6: 69,376,946 (GRCm39) |
W68R |
probably damaging |
Het |
Il23r |
A |
G |
6: 67,443,401 (GRCm39) |
I234T |
probably damaging |
Het |
Ints2 |
T |
A |
11: 86,112,963 (GRCm39) |
I852F |
probably damaging |
Het |
Ints2 |
G |
A |
11: 86,115,941 (GRCm39) |
Q763* |
probably null |
Het |
Jhy |
T |
G |
9: 40,872,182 (GRCm39) |
H109P |
probably benign |
Het |
Katna1 |
T |
A |
10: 7,614,579 (GRCm39) |
V29D |
possibly damaging |
Het |
Kcng4 |
T |
A |
8: 120,352,970 (GRCm39) |
E313D |
probably benign |
Het |
Klf14 |
T |
A |
6: 30,935,049 (GRCm39) |
H195L |
probably damaging |
Het |
Lama3 |
A |
G |
18: 12,554,212 (GRCm39) |
N472S |
probably benign |
Het |
Layn |
A |
T |
9: 50,970,781 (GRCm39) |
V254E |
possibly damaging |
Het |
Lrba |
A |
T |
3: 86,283,235 (GRCm39) |
S1850C |
probably damaging |
Het |
Map1s |
A |
G |
8: 71,358,909 (GRCm39) |
I2V |
unknown |
Het |
Map3k12 |
T |
A |
15: 102,413,797 (GRCm39) |
Q58L |
possibly damaging |
Het |
Minpp1 |
T |
C |
19: 32,491,396 (GRCm39) |
V358A |
probably benign |
Het |
Mymk |
C |
G |
2: 26,961,947 (GRCm39) |
K27N |
possibly damaging |
Het |
Nek8 |
T |
C |
11: 78,063,375 (GRCm39) |
K130E |
probably damaging |
Het |
Ngef |
T |
A |
1: 87,405,293 (GRCm39) |
S706C |
probably damaging |
Het |
Nsun6 |
G |
A |
2: 15,001,306 (GRCm39) |
Q417* |
probably null |
Het |
Ntsr2 |
G |
T |
12: 16,706,852 (GRCm39) |
Q293H |
probably damaging |
Het |
Ocln |
T |
A |
13: 100,676,050 (GRCm39) |
I148F |
probably damaging |
Het |
Or12d12 |
A |
G |
17: 37,610,701 (GRCm39) |
I204T |
probably benign |
Het |
Or4p19 |
A |
T |
2: 88,242,091 (GRCm39) |
Y304N |
probably benign |
Het |
Or8g30 |
T |
A |
9: 39,229,989 (GRCm39) |
Q307L |
probably benign |
Het |
Pank3 |
T |
G |
11: 35,672,412 (GRCm39) |
F272V |
probably damaging |
Het |
Piezo1 |
A |
T |
8: 123,223,328 (GRCm39) |
|
probably benign |
Het |
Plppr4 |
G |
A |
3: 117,116,190 (GRCm39) |
R556* |
probably null |
Het |
Polr1a |
G |
T |
6: 71,927,612 (GRCm39) |
R821L |
probably benign |
Het |
Ppp1r36 |
C |
T |
12: 76,485,967 (GRCm39) |
T375I |
probably benign |
Het |
Ptprj |
T |
A |
2: 90,290,856 (GRCm39) |
I628F |
possibly damaging |
Het |
Puf60 |
C |
A |
15: 75,949,525 (GRCm39) |
V29F |
unknown |
Het |
R3hdm2 |
T |
G |
10: 127,293,521 (GRCm39) |
S142A |
probably damaging |
Het |
Rassf1 |
A |
G |
9: 107,435,041 (GRCm39) |
S179G |
probably benign |
Het |
Rbm6 |
A |
G |
9: 107,665,337 (GRCm39) |
S772P |
possibly damaging |
Het |
Rnf103 |
T |
G |
6: 71,486,982 (GRCm39) |
S538A |
probably benign |
Het |
Scoc |
C |
A |
8: 84,164,245 (GRCm39) |
V58L |
probably benign |
Het |
Secisbp2l |
G |
A |
2: 125,602,263 (GRCm39) |
Q366* |
probably null |
Het |
Slc16a14 |
T |
C |
1: 84,890,784 (GRCm39) |
T174A |
probably benign |
Het |
Slc25a22 |
A |
C |
7: 141,011,020 (GRCm39) |
*324G |
probably null |
Het |
Smarca2 |
C |
T |
19: 26,753,558 (GRCm39) |
T197I |
probably benign |
Het |
Srgap2 |
T |
A |
1: 131,223,212 (GRCm39) |
N858I |
unknown |
Het |
Syna |
C |
T |
5: 134,588,723 (GRCm39) |
M75I |
probably benign |
Het |
Tbc1d22b |
T |
C |
17: 29,818,918 (GRCm39) |
I424T |
probably damaging |
Het |
Tcaf1 |
T |
G |
6: 42,656,221 (GRCm39) |
T252P |
probably benign |
Het |
Thbs1 |
A |
G |
2: 117,943,613 (GRCm39) |
D77G |
probably damaging |
Het |
Tlcd3a |
T |
C |
11: 76,098,941 (GRCm39) |
F237S |
probably damaging |
Het |
Trim21 |
T |
C |
7: 102,208,675 (GRCm39) |
E348G |
probably benign |
Het |
Trpm3 |
A |
G |
19: 22,896,040 (GRCm39) |
D959G |
probably benign |
Het |
Ttc24 |
A |
T |
3: 87,980,033 (GRCm39) |
C182* |
probably null |
Het |
Tti1 |
T |
C |
2: 157,850,514 (GRCm39) |
T242A |
probably benign |
Het |
Ube2q2l |
G |
A |
6: 136,378,729 (GRCm39) |
Q34* |
probably null |
Het |
Ube3b |
G |
T |
5: 114,526,800 (GRCm39) |
C100F |
probably damaging |
Het |
Vmn1r26 |
T |
A |
6: 57,985,440 (GRCm39) |
T250S |
possibly damaging |
Het |
Vnn1 |
A |
G |
10: 23,780,526 (GRCm39) |
T505A |
probably benign |
Het |
Vps13a |
C |
A |
19: 16,642,153 (GRCm39) |
W2158L |
probably damaging |
Het |
Vwa1 |
A |
T |
4: 155,857,345 (GRCm39) |
V151E |
probably damaging |
Het |
Zfp14 |
A |
G |
7: 29,742,961 (GRCm39) |
S46P |
probably damaging |
Het |
Zfp773 |
C |
A |
7: 7,135,570 (GRCm39) |
C342F |
probably benign |
Het |
Zscan12 |
T |
A |
13: 21,547,991 (GRCm39) |
S58T |
possibly damaging |
Het |
|
Other mutations in Speg |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00838:Speg
|
APN |
1 |
75,387,034 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL00979:Speg
|
APN |
1 |
75,387,378 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01122:Speg
|
APN |
1 |
75,386,679 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01293:Speg
|
APN |
1 |
75,364,746 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01304:Speg
|
APN |
1 |
75,404,841 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01351:Speg
|
APN |
1 |
75,387,920 (GRCm39) |
splice site |
probably benign |
|
IGL01473:Speg
|
APN |
1 |
75,404,929 (GRCm39) |
missense |
possibly damaging |
0.53 |
IGL01477:Speg
|
APN |
1 |
75,368,541 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01485:Speg
|
APN |
1 |
75,364,471 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01584:Speg
|
APN |
1 |
75,407,581 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01959:Speg
|
APN |
1 |
75,367,734 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02231:Speg
|
APN |
1 |
75,400,031 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02355:Speg
|
APN |
1 |
75,400,559 (GRCm39) |
missense |
possibly damaging |
0.49 |
IGL02362:Speg
|
APN |
1 |
75,400,559 (GRCm39) |
missense |
possibly damaging |
0.49 |
IGL03013:Speg
|
APN |
1 |
75,407,923 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL03168:Speg
|
APN |
1 |
75,364,831 (GRCm39) |
missense |
probably damaging |
1.00 |
H8562:Speg
|
UTSW |
1 |
75,392,241 (GRCm39) |
missense |
probably benign |
0.39 |
R0112:Speg
|
UTSW |
1 |
75,361,676 (GRCm39) |
missense |
possibly damaging |
0.92 |
R0311:Speg
|
UTSW |
1 |
75,407,581 (GRCm39) |
missense |
probably damaging |
1.00 |
R0315:Speg
|
UTSW |
1 |
75,391,780 (GRCm39) |
missense |
possibly damaging |
0.88 |
R0393:Speg
|
UTSW |
1 |
75,400,568 (GRCm39) |
missense |
possibly damaging |
0.46 |
R0403:Speg
|
UTSW |
1 |
75,407,428 (GRCm39) |
splice site |
probably benign |
|
R0483:Speg
|
UTSW |
1 |
75,361,676 (GRCm39) |
missense |
possibly damaging |
0.92 |
R0648:Speg
|
UTSW |
1 |
75,404,622 (GRCm39) |
missense |
probably benign |
|
R0683:Speg
|
UTSW |
1 |
75,405,762 (GRCm39) |
missense |
probably damaging |
1.00 |
R0800:Speg
|
UTSW |
1 |
75,400,133 (GRCm39) |
missense |
probably damaging |
1.00 |
R0815:Speg
|
UTSW |
1 |
75,392,036 (GRCm39) |
missense |
probably damaging |
1.00 |
R0835:Speg
|
UTSW |
1 |
75,352,318 (GRCm39) |
missense |
probably benign |
0.00 |
R0866:Speg
|
UTSW |
1 |
75,393,727 (GRCm39) |
missense |
probably damaging |
0.99 |
R0880:Speg
|
UTSW |
1 |
75,381,705 (GRCm39) |
missense |
probably damaging |
1.00 |
R1082:Speg
|
UTSW |
1 |
75,391,782 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1140:Speg
|
UTSW |
1 |
75,405,739 (GRCm39) |
missense |
probably damaging |
1.00 |
R1252:Speg
|
UTSW |
1 |
75,403,739 (GRCm39) |
missense |
probably damaging |
1.00 |
R1301:Speg
|
UTSW |
1 |
75,378,145 (GRCm39) |
missense |
probably damaging |
1.00 |
R1348:Speg
|
UTSW |
1 |
75,399,516 (GRCm39) |
missense |
probably damaging |
0.99 |
R1388:Speg
|
UTSW |
1 |
75,407,104 (GRCm39) |
missense |
probably damaging |
0.99 |
R1465:Speg
|
UTSW |
1 |
75,405,128 (GRCm39) |
splice site |
probably benign |
|
R1505:Speg
|
UTSW |
1 |
75,352,186 (GRCm39) |
missense |
probably benign |
0.02 |
R1506:Speg
|
UTSW |
1 |
75,394,307 (GRCm39) |
missense |
probably benign |
0.03 |
R1531:Speg
|
UTSW |
1 |
75,377,866 (GRCm39) |
missense |
possibly damaging |
0.86 |
R1543:Speg
|
UTSW |
1 |
75,398,595 (GRCm39) |
missense |
probably damaging |
1.00 |
R1567:Speg
|
UTSW |
1 |
75,404,691 (GRCm39) |
missense |
probably benign |
|
R1630:Speg
|
UTSW |
1 |
75,399,621 (GRCm39) |
missense |
probably damaging |
1.00 |
R1667:Speg
|
UTSW |
1 |
75,387,193 (GRCm39) |
splice site |
probably benign |
|
R1673:Speg
|
UTSW |
1 |
75,387,807 (GRCm39) |
missense |
possibly damaging |
0.60 |
R1718:Speg
|
UTSW |
1 |
75,398,388 (GRCm39) |
missense |
possibly damaging |
0.87 |
R1718:Speg
|
UTSW |
1 |
75,394,507 (GRCm39) |
missense |
probably benign |
0.00 |
R1719:Speg
|
UTSW |
1 |
75,394,507 (GRCm39) |
missense |
probably benign |
0.00 |
R1759:Speg
|
UTSW |
1 |
75,377,806 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1861:Speg
|
UTSW |
1 |
75,365,649 (GRCm39) |
missense |
probably damaging |
1.00 |
R1874:Speg
|
UTSW |
1 |
75,400,550 (GRCm39) |
missense |
probably benign |
|
R1936:Speg
|
UTSW |
1 |
75,408,052 (GRCm39) |
missense |
possibly damaging |
0.93 |
R2192:Speg
|
UTSW |
1 |
75,394,371 (GRCm39) |
missense |
probably damaging |
1.00 |
R2204:Speg
|
UTSW |
1 |
75,407,121 (GRCm39) |
missense |
probably benign |
0.30 |
R2287:Speg
|
UTSW |
1 |
75,407,109 (GRCm39) |
missense |
possibly damaging |
0.76 |
R2696:Speg
|
UTSW |
1 |
75,383,570 (GRCm39) |
missense |
probably benign |
0.27 |
R2983:Speg
|
UTSW |
1 |
75,361,574 (GRCm39) |
missense |
possibly damaging |
0.83 |
R3110:Speg
|
UTSW |
1 |
75,399,326 (GRCm39) |
nonsense |
probably null |
|
R3112:Speg
|
UTSW |
1 |
75,399,326 (GRCm39) |
nonsense |
probably null |
|
R3154:Speg
|
UTSW |
1 |
75,378,186 (GRCm39) |
missense |
probably damaging |
1.00 |
R3720:Speg
|
UTSW |
1 |
75,403,426 (GRCm39) |
missense |
probably damaging |
1.00 |
R3983:Speg
|
UTSW |
1 |
75,399,191 (GRCm39) |
missense |
probably benign |
0.27 |
R4133:Speg
|
UTSW |
1 |
75,404,548 (GRCm39) |
missense |
probably benign |
|
R4522:Speg
|
UTSW |
1 |
75,404,974 (GRCm39) |
missense |
probably damaging |
1.00 |
R4564:Speg
|
UTSW |
1 |
75,368,478 (GRCm39) |
missense |
probably damaging |
1.00 |
R4577:Speg
|
UTSW |
1 |
75,392,039 (GRCm39) |
missense |
probably damaging |
1.00 |
R4858:Speg
|
UTSW |
1 |
75,398,379 (GRCm39) |
missense |
probably damaging |
1.00 |
R4953:Speg
|
UTSW |
1 |
75,400,508 (GRCm39) |
missense |
possibly damaging |
0.72 |
R4965:Speg
|
UTSW |
1 |
75,404,347 (GRCm39) |
missense |
probably damaging |
1.00 |
R4967:Speg
|
UTSW |
1 |
75,364,513 (GRCm39) |
missense |
probably damaging |
1.00 |
R5152:Speg
|
UTSW |
1 |
75,404,742 (GRCm39) |
missense |
possibly damaging |
0.92 |
R5156:Speg
|
UTSW |
1 |
75,404,731 (GRCm39) |
missense |
probably damaging |
0.99 |
R5371:Speg
|
UTSW |
1 |
75,408,037 (GRCm39) |
missense |
possibly damaging |
0.50 |
R5550:Speg
|
UTSW |
1 |
75,405,744 (GRCm39) |
missense |
probably damaging |
1.00 |
R5562:Speg
|
UTSW |
1 |
75,403,700 (GRCm39) |
missense |
probably damaging |
1.00 |
R5687:Speg
|
UTSW |
1 |
75,395,773 (GRCm39) |
splice site |
probably null |
|
R5985:Speg
|
UTSW |
1 |
75,383,328 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6004:Speg
|
UTSW |
1 |
75,392,247 (GRCm39) |
nonsense |
probably null |
|
R6038:Speg
|
UTSW |
1 |
75,395,103 (GRCm39) |
critical splice donor site |
probably null |
|
R6038:Speg
|
UTSW |
1 |
75,395,103 (GRCm39) |
critical splice donor site |
probably null |
|
R6143:Speg
|
UTSW |
1 |
75,391,031 (GRCm39) |
missense |
probably damaging |
1.00 |
R6265:Speg
|
UTSW |
1 |
75,383,323 (GRCm39) |
nonsense |
probably null |
|
R6347:Speg
|
UTSW |
1 |
75,403,519 (GRCm39) |
missense |
probably benign |
0.00 |
R6453:Speg
|
UTSW |
1 |
75,394,616 (GRCm39) |
missense |
probably benign |
0.06 |
R6505:Speg
|
UTSW |
1 |
75,406,167 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6505:Speg
|
UTSW |
1 |
75,383,328 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6531:Speg
|
UTSW |
1 |
75,399,401 (GRCm39) |
missense |
probably benign |
0.03 |
R6566:Speg
|
UTSW |
1 |
75,365,107 (GRCm39) |
missense |
probably damaging |
1.00 |
R6747:Speg
|
UTSW |
1 |
75,387,039 (GRCm39) |
critical splice donor site |
probably null |
|
R6819:Speg
|
UTSW |
1 |
75,368,456 (GRCm39) |
missense |
possibly damaging |
0.56 |
R6821:Speg
|
UTSW |
1 |
75,394,547 (GRCm39) |
missense |
possibly damaging |
0.83 |
R6919:Speg
|
UTSW |
1 |
75,364,552 (GRCm39) |
nonsense |
probably null |
|
R6981:Speg
|
UTSW |
1 |
75,407,557 (GRCm39) |
missense |
probably damaging |
1.00 |
R7002:Speg
|
UTSW |
1 |
75,399,912 (GRCm39) |
missense |
probably damaging |
0.98 |
R7082:Speg
|
UTSW |
1 |
75,388,091 (GRCm39) |
missense |
probably damaging |
0.96 |
R7140:Speg
|
UTSW |
1 |
75,383,414 (GRCm39) |
critical splice donor site |
probably null |
|
R7175:Speg
|
UTSW |
1 |
75,399,134 (GRCm39) |
missense |
probably benign |
0.01 |
R7178:Speg
|
UTSW |
1 |
75,399,027 (GRCm39) |
missense |
possibly damaging |
0.46 |
R7345:Speg
|
UTSW |
1 |
75,361,479 (GRCm39) |
missense |
probably damaging |
0.97 |
R7420:Speg
|
UTSW |
1 |
75,407,549 (GRCm39) |
missense |
probably damaging |
1.00 |
R7537:Speg
|
UTSW |
1 |
75,378,108 (GRCm39) |
missense |
probably damaging |
1.00 |
R7562:Speg
|
UTSW |
1 |
75,407,923 (GRCm39) |
missense |
probably damaging |
0.97 |
R7615:Speg
|
UTSW |
1 |
75,405,886 (GRCm39) |
missense |
probably damaging |
1.00 |
R7679:Speg
|
UTSW |
1 |
75,382,959 (GRCm39) |
missense |
probably damaging |
1.00 |
R7692:Speg
|
UTSW |
1 |
75,377,834 (GRCm39) |
missense |
probably benign |
0.04 |
R7696:Speg
|
UTSW |
1 |
75,405,805 (GRCm39) |
missense |
probably damaging |
1.00 |
R7719:Speg
|
UTSW |
1 |
75,352,469 (GRCm39) |
missense |
probably damaging |
1.00 |
R7794:Speg
|
UTSW |
1 |
75,365,514 (GRCm39) |
missense |
probably benign |
0.00 |
R7824:Speg
|
UTSW |
1 |
75,360,661 (GRCm39) |
splice site |
probably null |
|
R7834:Speg
|
UTSW |
1 |
75,361,571 (GRCm39) |
missense |
probably damaging |
1.00 |
R7892:Speg
|
UTSW |
1 |
75,403,810 (GRCm39) |
missense |
probably damaging |
1.00 |
R8015:Speg
|
UTSW |
1 |
75,392,065 (GRCm39) |
splice site |
probably benign |
|
R8068:Speg
|
UTSW |
1 |
75,398,894 (GRCm39) |
missense |
probably damaging |
1.00 |
R8085:Speg
|
UTSW |
1 |
75,391,997 (GRCm39) |
missense |
probably damaging |
1.00 |
R8130:Speg
|
UTSW |
1 |
75,392,240 (GRCm39) |
missense |
probably damaging |
1.00 |
R8132:Speg
|
UTSW |
1 |
75,399,639 (GRCm39) |
missense |
probably damaging |
1.00 |
R8239:Speg
|
UTSW |
1 |
75,395,677 (GRCm39) |
missense |
probably damaging |
1.00 |
R8287:Speg
|
UTSW |
1 |
75,398,880 (GRCm39) |
missense |
probably benign |
0.26 |
R8299:Speg
|
UTSW |
1 |
75,364,480 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8441:Speg
|
UTSW |
1 |
75,387,976 (GRCm39) |
missense |
possibly damaging |
0.60 |
R8468:Speg
|
UTSW |
1 |
75,407,953 (GRCm39) |
missense |
probably damaging |
1.00 |
R8555:Speg
|
UTSW |
1 |
75,378,908 (GRCm39) |
splice site |
probably null |
|
R8781:Speg
|
UTSW |
1 |
75,383,665 (GRCm39) |
missense |
probably damaging |
1.00 |
R8848:Speg
|
UTSW |
1 |
75,404,082 (GRCm39) |
critical splice donor site |
probably null |
|
R8881:Speg
|
UTSW |
1 |
75,377,795 (GRCm39) |
missense |
possibly damaging |
0.67 |
R8898:Speg
|
UTSW |
1 |
75,365,517 (GRCm39) |
missense |
probably damaging |
1.00 |
R8935:Speg
|
UTSW |
1 |
75,399,250 (GRCm39) |
missense |
probably benign |
0.30 |
R9019:Speg
|
UTSW |
1 |
75,405,882 (GRCm39) |
missense |
probably damaging |
1.00 |
R9027:Speg
|
UTSW |
1 |
75,365,076 (GRCm39) |
missense |
possibly damaging |
0.67 |
R9066:Speg
|
UTSW |
1 |
75,361,654 (GRCm39) |
missense |
probably damaging |
0.99 |
R9092:Speg
|
UTSW |
1 |
75,399,378 (GRCm39) |
missense |
probably benign |
0.01 |
R9117:Speg
|
UTSW |
1 |
75,364,444 (GRCm39) |
missense |
probably damaging |
1.00 |
R9202:Speg
|
UTSW |
1 |
75,367,637 (GRCm39) |
missense |
probably damaging |
1.00 |
R9246:Speg
|
UTSW |
1 |
75,361,498 (GRCm39) |
missense |
probably damaging |
1.00 |
R9248:Speg
|
UTSW |
1 |
75,398,420 (GRCm39) |
missense |
probably damaging |
1.00 |
R9451:Speg
|
UTSW |
1 |
75,394,377 (GRCm39) |
missense |
probably damaging |
1.00 |
R9452:Speg
|
UTSW |
1 |
75,399,152 (GRCm39) |
missense |
probably benign |
|
R9475:Speg
|
UTSW |
1 |
75,364,735 (GRCm39) |
missense |
probably damaging |
1.00 |
R9476:Speg
|
UTSW |
1 |
75,377,768 (GRCm39) |
missense |
probably damaging |
0.99 |
R9510:Speg
|
UTSW |
1 |
75,377,768 (GRCm39) |
missense |
probably damaging |
0.99 |
R9519:Speg
|
UTSW |
1 |
75,392,380 (GRCm39) |
missense |
probably damaging |
1.00 |
R9528:Speg
|
UTSW |
1 |
75,364,447 (GRCm39) |
missense |
possibly damaging |
0.78 |
R9542:Speg
|
UTSW |
1 |
75,399,426 (GRCm39) |
missense |
probably benign |
0.08 |
R9553:Speg
|
UTSW |
1 |
75,394,645 (GRCm39) |
missense |
probably benign |
0.00 |
R9767:Speg
|
UTSW |
1 |
75,403,825 (GRCm39) |
missense |
possibly damaging |
0.78 |
R9768:Speg
|
UTSW |
1 |
75,395,617 (GRCm39) |
nonsense |
probably null |
|
R9800:Speg
|
UTSW |
1 |
75,399,358 (GRCm39) |
missense |
probably benign |
0.03 |
X0025:Speg
|
UTSW |
1 |
75,399,101 (GRCm39) |
missense |
probably damaging |
1.00 |
X0026:Speg
|
UTSW |
1 |
75,400,119 (GRCm39) |
missense |
possibly damaging |
0.88 |
Z1176:Speg
|
UTSW |
1 |
75,383,238 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Speg
|
UTSW |
1 |
75,404,327 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Speg
|
UTSW |
1 |
75,407,099 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1177:Speg
|
UTSW |
1 |
75,405,025 (GRCm39) |
missense |
probably damaging |
1.00 |
|